Symbol Name ID |
Rdh12
retinol dehydrogenase 12 MGI:1925224 |
Darker colors indicate more annotations |
Human Phenotypes | Central retinal vessel vascular tortuosity |
Attenuation of retinal blood vessels |
Optic atrophy |
Optic disc pallor |
Leber optic atrophy |
Optic neuropathy |
Bone spicule pigmentation of the retina |
Retinal dystrophy |
Reduced visual acuity |
Centrocecal scotoma |
Visual loss |
Disease(s) Associated with RDH12 | |||||||||||
Leber congenital amaurosis 13 | |||||||||||
Leber hereditary optic neuropathy |
Mouse Phenotypes | abnormal retina apoptosis |
short retina rod cell outer segment |
abnormal retina neuronal layer morphology |
abnormal eye physiology |
abnormal eye electrophysiology |
delayed dark adaptation |
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Availability | Mouse Genotype | ||||||
Rdh12tm1.1Cahb/Rdh12tm1.1Cahb | |||||||
Rdh12tm1Kpal/Rdh12tm1Kpal | |||||||
Rdh12tm1Kpal/Rdh12+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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